Reliability Engineering Lead – GMP Pharma

Simtra US LLC; Bloomington (IN); On-site; USD 120,000 - 160,000; Full time

Benefits offered by this job

Medical & Dental Coverage

401(k) Retirement Savings Plan with 1:

Paid Time Off

Education Assistance Program

Job summary

Simtra BioPharma Solutions is seeking an Associate Director of Reliability Engineering in Bloomington, IN. The role leads the site reliability program to maximize equipment uptime, RTS performance, asset performance, product quality, safety, and regulatory compliance within a GMP environment.

You will partner with Engineering, Manufacturing, Quality, Validation, Facilities, Supply Chain, and EHS to ensure reliable operation of GMP-regulated systems while supporting capital plans and production

Qualifications

• Bachelor's degree in Engineering required.
• Master's degree in Engineering, MBA or related field preferred.
• 10+ years in engineering, maintenance, or reliability in pharma/regulated manufacturing.
• 5+ years of leadership experience managing technical teams.

Responsibilities

• Develop and execute the site Reliability Engineering strategy aligned with business and operational goals.
• Lead reliability improvement initiatives across manufacturing equipment, utilities, and facilities.
• Establish reliability standards, policies, and best practices.
• Provide data analytics and dashboards to monitor reliability performance and drive continuous improvement.

Skills

Reliability Engineering

Maintenance optimization

Predictive maintenance

RCM

OEE

Education

Bachelor's degree in Engineering

Master's degree preferred

Tools

CMMS (Maximo, D365, Blue Mountain)

Job description

Simtra BioPharma Solutions is seeking an Associate Director of Reliability Engineering in Bloomington, IN. The role leads the site reliability program to maximize equipment uptime, RTS performance, asset performance, product quality, safety, and regulatory compliance within a GMP environment.

You will partner with Engineering, Manufacturing, Quality, Validation, Facilities, Supply Chain, and EHS to ensure reliable operation of GMP-regulated systems while supporting capital plans and production